Canonical Allele Identifier: CA1543080392
Gene: FGF10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305635_44305637delinsCTT , CM000667.2:g.44305635_44305637delinsCTT GRCh38
NC_000005.9:g.44305737_44305739delinsCTT , CM000667.1:g.44305737_44305739delinsCTT GRCh37
NC_000005.8:g.44341494_44341496delinsCTT NCBI36
NG_011446.1:g.88046_88048delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-445_430-443delinsAAG MANE Select ENSP00000264664.4:n.430-445_430-443delinsAAG
ENST00000264664.4:c.430-445_430-443delinsAAG ENSP00000264664.4:n.430-445_430-443delinsAAG
NM_004465.1:c.430-445_430-443delinsAAG NP_004456.1:n.430-445_430-443delinsAAG
XM_005248264.2:c.430-445_430-443delinsAAG XP_005248321.1:n.430-445_430-443delinsAAG
XM_005248264.4:c.430-445_430-443delinsAAG XP_005248321.1:n.430-445_430-443delinsAAG
NM_004465.2:c.430-445_430-443delinsAAG MANE Select NP_004456.1:n.430-445_430-443delinsAAG
Search 100 bp 5'
Search 100 bp 3'